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rs1060502640

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502640(-;-)
Make rs1060502640(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32287614
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502640
dbSNP (old)rs1060502640
ClinGenrs1060502640
ebirs1060502640
HLIrs1060502640
Exacrs1060502640
Gnomadrs1060502640
Varsomers1060502640
Maprs1060502640
PheGenIrs1060502640
Biobankrs1060502640
1000 genomesrs1060502640
hgdprs1060502640
ensemblrs1060502640
gopubmedrs1060502640
geneviewrs1060502640
scholarrs1060502640
googlers1060502640
pharmgkbrs1060502640
gwascentralrs1060502640
openSNPrs1060502640
23andMers1060502640
23andMe allrs1060502640
SNPshotrs1060502640
SNPdbers1060502640
MSV3drs1060502640
GWAS Ctlgrs1060502640
Max Magnitude0
ClinVar
Risk rs1060502640(-;-)
Alt rs1060502640(-;-)
Reference Rs1060502640(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32305731delC
CLNSRC
CLNACC RCV000466920.1,